A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17983008



Internal ID20550048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68308501..68309600hg38UCSC Ensembl
chr10:70068258..70069357hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445697
Supporting Variants
Samples
Known GenesPBLD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17983008
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.03368


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